US9815992B2

US9815992B2 - Acrylate ink compositions for ink-based digital lithographic printing

Info

Publication number: US9815992B2
Application number: US14/610,437
Authority: US
Inventors: C. Geoffrey Allen; Carolyn Moorlag; Mihaela Maria Birau; Aurelian Valeriu Magdalinis
Original assignee: Xerox Corp
Current assignee: Xerox Corp
Priority date: 2015-01-30
Filing date: 2015-01-30
Publication date: 2017-11-14
Anticipated expiration: 2035-01-30
Also published as: DE102016200537A1; JP2016141810A; US20160222231A1; DE102016200537B4; JP6864987B2

Abstract

An ink composition, including 30% or less pigment, 10% or less dispersant, between 40% and 80% acrylate, 12% or less photoinitiator, and having a viscosity between 2×10⁶cP and 5×10⁷cP at 25° C., and between 2.×10⁵cP and 4.×10⁶cP at 60° C., and a 60 second tack between 40 and 65 g-m at 25° C., and between 10 and 20 g-m at 60° C.

Description

FIELD OF DISCLOSURE

This disclosure relates to ink compositions for printing on substrates. In particular, the disclosure relates to acrylate ink compositions useful for digital lithographic printing systems.

BACKGROUND

In typical lithographic printing systems, a printing plate is formed to have “image regions” formed of a hydrophobic/oleophilic material and “non-image regions” formed of a hydrophilic/oleophobic material. The image regions correspond to the areas on the final print (i.e., the target substrate) that are occupied by ink, whereas the non-image regions correspond to the areas on the final print that are not occupied by said ink. The hydrophilic regions accept and are readily wetted by a water-based fluid, commonly referred to as a dampening fluid or fountain fluid (typically consisting of water and a small amount of alcohol as well as other additives and/or surfactants to reduce surface tension). The hydrophobic regions repel dampening fluid and accept ink, whereas the dampening fluid formed over the hydrophilic regions forms a fluid “release layer” for rejecting ink. The hydrophilic regions of the printing plate thus correspond to unprinted areas, or “non-image areas”, of the final print.

The ink may be transferred directly to a target substrate, such as paper, or may be applied to an intermediate surface, such as an offset (or blanket) cylinder in an offset printing system.

Typical lithographic and offset printing techniques utilize plates which are permanently patterned, and are therefore useful only when printing a large number of copies of the same image (i.e. long print runs), such as magazines, newspapers, and the like. However, variable data digital lithography or digital offset lithography has been developed as a system which uses a non-patterned reimageable surface that is initially uniformly coated with a dampening fluid layer. Regions of the dampening fluid are removed by exposure to a focused radiation source (e.g., a laser light source) to form pockets. A temporary pattern in the dampening fluid is thereby formed over the non-patterned reimageable surface. Ink applied thereover is retained in the pockets formed by the removal of the dampening fluid. The inked surface is then brought into contact with a substrate, and the ink transfers from the pockets in the dampening fluid layer to the substrate. The dampening fluid may then be removed, a new uniform layer of dampening fluid applied to the reimageable surface, and the process repeated.

Digital offset lithography printing systems use offset-type inks that are specifically designed and optimized to be compatible with various subsystems, including ink delivery systems and a laser imaging systems, to enable high quality digital printing at high speed. Related art offset-type inks suffer shortfalls including, but not limited to, (1) being difficult to deliver via preferred inking systems, including anilox roller-type inking systems, (2) being soluble in commonly-employed dampening fluids, such as octamethylcyclotetrasiloxane (D4), (3) causing image background and/or ghosting issues, (4) being costly to manufacture and use, and (5) exhibiting inefficient image transfer. These shortfalls, individually and in combination, tend to narrow a design space within which related art inks are usable in the context of digital offset lithography printing systems.

SUMMARY

Accordingly, there is a need to develop inks that exhibit improved qualities and that may address one or all of the above-identified shortfalls. Extensive experimentation has revealed that acrylate ink compositions according to embodiments of this disclosure may provide enhanced ease of delivery to an imaging member, such as a reimageable offset plate, enhanced transfer efficiency from the reimageable offset plate, and enhanced print quality on a variety of substrates. Further, these ink compositions do not tend to degrade printing system components, such as reimageable surfaces of imaging members, with which they contact. These acrylate ink compositions should meet various sub-system requirements imposed by ink-based digital printing systems that are configured for variable data lithographic printing. These requirements include wettability, releasability from a reimageable surface of an imaging member, and compatibility with non-aqueous dampening fluids configured for use with ink-based digital printing methods and systems.

Acrylate ink compositions are provided herein that meet the foregoing requirements. The disclosed acrylate ink compositions may be effectively delivered from an anilox roller-type delivery system to a reimageable surface of an imaging member during a variable data offset printing operation in which images on the reimageable surface are changeable between cycles of the imaging member. The disclosed acrylate ink compositions exhibit stable rheology that enables delivery using an anilox roll delivery system, and demonstrate desirable transferability to a reimageable surface of an imaging member.

The following presents a simplified summary in order to provide a basic understanding of some aspects of one or more embodiments of the present teachings. This summary is not an extensive overview, nor is it intended to identify key or critical elements of the present teachings, nor to delineate the scope of the disclosure. Rather, its primary purpose is merely to present one or more concepts in simplified form as a prelude to the detailed description presented later.

Additional goals and advantages will become more evident in the description of the figures, the detailed description of the disclosure, and the claims.

The foregoing and/or other aspects and utilities embodied in the present disclosure may be achieved by providing an ink composition, including 30% or less by weight pigment, based on a total weight of the ink composition; 10% or less by weight dispersant, based on the total weight of the ink composition; between 40% and 80% by weight acrylate, based on the total weight of the ink composition; and 12% or less by weight photoinitiator, based on the total weight of the ink composition, wherein a viscosity of the ink composition is between 2×10⁶cP and 5×10⁷cP at 25° C., and between 2×10⁵cP and 4×10⁶cP at 60° C., and wherein a 60 second tack of the ink composition is between 40 g-m and 65 g-m at 25° C., and between 10 g-m and 20 g-m at 60° C.

In another embodiment, the ink composition further includes 1.5% or less by weight stabilizer, based on the total weight of the ink composition; and 12% or less by weight rheology modifier, based on the total weight of the ink composition.

In another embodiment, the ink composition includes between 15% and 20% pigment; between 4% and 8% dispersant; between 60% and 70% acrylate; between 5% and 10% photoinitiator; between 0.1% and 0.3% stabilizer; and 3% or less rheology modifier, wherein the ink composition has a viscosity between 4×10⁶cP and 1×10⁷cP at 25° C., and between 4×10⁵cP and 8×10⁵cP at 60° C., and wherein a 60 second tack of the ink composition is between 45 g-m and 55 g-m at 25° C., and between 10 g-m and 15 g-m at 60° C.

In another embodiment, the acrylate comprises at least one of an acrylate monomer, acrylate polymer, acrylate oligomer, a trifunctional acrylate monomer, a polyester acrylate, and mixtures thereof.

The foregoing and/or other aspects and utilities embodied in the present disclosure may be achieved by providing an ink composition, essentially consisting of 30% or less by weight pigment, based on a total weight of the ink composition; 10% or less by weight dispersant, based on the total weight of the ink composition; between 40% and 80% by weight acrylate, based on the total weight of the ink composition; 12% or less by weight photoinitiator, based on the total weight of the ink composition; 1.5% or less by weight stabilizer, based on the total weight of the ink composition; and 12% or less by weight rheology modifier, based on the total weight of the ink composition, wherein a viscosity of the ink composition is between 2×10⁸cP and 5×10⁷cP at 25° C., and between 2.×10⁵cP and 4.×10⁶cP at 60° C., and wherein a 60 second tack of the ink composition is between 40 g-m and 65 g-m at 25° C., and between 10 g-m and 20 g-m at 60° C.

The foregoing and/or other aspects and utilities embodied in the present disclosure may be achieved by providing a method of printing using a variable data digital lithographic printing device, including applying an ink composition to a reimageable surface of an imaging member; and transferring the ink composition from the reimageable surface to a substrate, wherein the ink composition does not require pre-curing before transferring the ink composition from the reimageable surface to the substrate, and wherein the ink composition comprises 30% or less by weight pigment, based on a total weight of the ink composition; 10% or less by weight dispersant, based on the total weight of the ink composition; between 40% and 80% by weight acrylate, based on the total weight of the ink composition; 12% or less by weight photoinitiator, based on the total weight of the ink composition; 1.5% or less by weight stabilizer, based on the total weight of the ink composition; and 12% or less by weight rheology modifier, based on the total weight of the ink composition, wherein a viscosity of the ink composition is between 2×10⁶cP and 5×10⁷cP at 25° C., and between 2.×10⁵cP and 4.×10⁶cP at 60° C., and wherein a 60 second tack of the ink composition is between 40 and 65 g-m at 25° C., and between 10 and 20 g-m at 60° C.

In another embodiment, the ink composition consists essentially of between 15% and 20% pigment; between 4% and 8% dispersant; between 60% and 70% acrylate; between 5% and 10% photoinitiator; between 0.1% and 0.3% stabilizer; and 3% or less rheology modifier.

In another embodiment, the ink composition has a viscosity between 4×10⁶cP and 1×10⁷cP at 25° C., and between 4×10⁵cP and 8×10⁵cP at 60° C., and wherein a 60 second tack of the ink composition is between 45 g-m and 55 g-m at 25° C., and between 10 g-m and 15 g-m at 60° C.

In another embodiment, the acrylate includes at least one of an acrylate monomer, acrylate polymer, acrylate oligomer, a trifunctional acrylate monomer, a polyester acrylate, and mixtures thereof.

The foregoing and/or other aspects and utilities embodied in the present disclosure may be achieved by providing a method of printing using a variable data digital lithographic printing device, including applying an ink composition at a first temperature to a reimageable surface of an imaging member; and transferring the ink composition from the reimageable surface to a substrate at a second temperature, wherein the ink composition does not require pre-curing before transferring the ink composition from the reimageable surface to the substrate, wherein the ink composition includes 30% or less by weight pigment, based on a total weight of the ink composition; 10% or less by weight dispersant, based on the total weight of the ink composition; between 40% and 80% by weight acrylate, based on the total weight of the ink composition; and 12% or less by weight photoinitiator, based on the total weight of the ink composition, wherein a viscosity of the ink composition is lower at the first temperature then at the second temperature, and wherein a 60 second tack of the ink composition is lower at the first temperature then at the second temperature.

In another embodiment, the second temperature is between 25° C. and 60° C., the second temperature is lower than the first temperature, and the 60 second tack of the acrylate ink composition at the second temperature is about 1.3 times lower per about 7-8° C. increase from the first temperature.

In another embodiment, the second temperature is between 25° C. and 60° C., the second temperature is lower than the first temperature, and the viscosity of the acrylate ink composition at the second temperature is about 1.2 times lower per about 10° C. increase from the first temperature.

In another embodiment, the first temperature is at least 20° C. higher than the second temperature.

In another embodiment, the first temperature is at least 50° C. higher than the second temperature.

In another embodiment, the first temperature is at least 80° C. higher than the second temperature.

In another embodiment, the ink has a viscosity between 2×10⁶cP and 5×10⁷cP at the second temperature ° C., and between 2.×10⁵cP and 4.×10⁶cP at the first temperature, and a 60 second tack of the ink composition is between 40 and 65 g-m at the second temperature, and between 10 and 20 g-m at the first temperature.

BRIEF DESCRIPTION OF THE DRAWINGS

These and/or other aspects and advantages in the embodiments of the disclosure will become apparent and more readily appreciated from the following description of the various embodiments, taken in conjunction with the accompanying drawings of which:

FIG. 1 illustrates a variable image digital printing system.

FIG. 2 illustrates frequency-based rheograms of acrylate ink compositions.

FIG. 3 illustrates tack results of acrylate ink compositions.

It should be noted that some details of the drawings have been simplified and are drawn to facilitate understanding of the present teachings rather than to maintain strict structural accuracy, detail, and scale.

The drawings above are not necessarily to scale, with emphasis instead generally being placed upon illustrating the principles in the present disclosure.

Further, some features may be exaggerated to show details of particular components. These drawings/figures are intended to be explanatory and not restrictive.

DETAILED DESCRIPTION

Reference will now be made in detail to the various embodiments in the present disclosure. The embodiments are described below to provide a more complete understanding of the components, processes and apparatuses disclosed herein. Any examples given are intended to be illustrative, and not restrictive. Throughout the specification and claims, the following terms take the meanings explicitly associated herein, unless the context clearly dictates otherwise. The phrases “in some embodiments” and “in an embodiment” as used herein do not necessarily refer to the same embodiment(s), though they may. Furthermore, the phrases “in another embodiment” and “in some other embodiments” as used herein do not necessarily refer to a different embodiment, although they may. As described below, various embodiments may be readily combined, without departing from the scope or spirit of the present disclosure.

As used herein, the term “or” is an inclusive operator, and is equivalent to the term “and/or,” unless the context clearly dictates otherwise. The term “based on” is not exclusive and allows for being based on additional factors not described, unless the context clearly dictates otherwise. In the specification, the recitation of “at least one of A, B, and C,” includes embodiments containing A, B, or C, multiple examples of A, B, or C, or combinations of A/B, A/C, B/C, A/B/B/B/B/C, A/B/C, etc. In addition, throughout the specification, the meaning of “a,” “an,” and “the” include plural references. The meaning of “in” includes “in” and “on.”

All physical properties that are defined hereinafter are measured at 20° to 25° Celsius unless otherwise specified. The term “room temperature” refers to 25° Celsius unless otherwise specified.

When referring to any numerical range of values herein, such ranges are understood to include each and every number and/or fraction between the stated range minimum and maximum. For example, a range of 0.5-6% would expressly include all intermediate values of 0.6%, 0.7%, and 0.9%, all the way up to and including 5.95%, 5.97%, and 5.99%. The same applies to each other numerical property and/or elemental range set forth herein, unless the context dearly dictates otherwise.

The present disclosure has been described with reference to exemplary embodiments. Although a few embodiments have been shown and described, it will be appreciated by those skilled in the art that changes may be made in these embodiments without departing from the principles and spirit of preceding detailed description. It is intended that the present disclosure be construed as including all such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof. For example, while the embodiments below are described in view of the printing system illustrated in FIG. 1, it should be understood that embodiments of the acrylate ink compositions described herein may also be used with other compatible printing systems.

Ink compositions in accordance with embodiments recited herein are suitable for ink-based digital printing. “Variable data lithography printing,” or “ink-based digital printing,” or “digital offset printing,” as these terms may be used throughout this disclosure, refer to lithographic printing of variable image data for producing images on a substrate that are changeable with each subsequent rendering of an image on the substrate in an image forming process. “Variable data lithographic printing” includes offset printing of ink images using lithographic ink where the images are based on digital image data that may vary from image to image. Ink-based digital printing uses a variable data lithography printing system or digital offset printing system. A “variable data lithography system” is a system that is configured for lithographic printing using lithographic inks and based on digital image data, which may vary from one image to the next.

By way of example, an ink-based digital printing system with anilox roll ink delivery subsystem that may be used with embodiments of the acrylate ink compositions herein is described in U.S. patent application Ser. No. 13/095,714. U.S. patent application Ser. No. 13/095,714 (“714 application”), titled “Variable Data Lithography System,” filed on Apr. 27, 2011, by Timothy Stowe et al., which is commonly assigned, and the disclosure of which is hereby Incorporated by reference herein in its entirety, describes an exemplary variable data lithography system 100 for ink-based digital printing in FIG. 1.

A general description of the exemplary printing system 100 shown in FIG. 1 is provided below. Additional details regarding individual components and/or subsystems shown in the exemplary system 100 of FIG. 1 may be found in the 714 application.

FIG. 1 illustrates a variable image digital printing system. As illustrated in FIG. 1, a printing system 100 may include an imaging member 110. While the imaging member 110 is illustrated in FIG. 1 as a drum, in other embodiments, the imaging member 110 could also be embodied as a plate, belt, or another now known or later developed configuration. The imaging member 110 includes a reimageable surface that may be formed of materials including, for example, a class of materials commonly referred to as silicones, including polydimethylsiloxane (PDMS), among others. For example, silicone, fluorosilicone, and/or fluoroelastomer may be used to form the reimageable surface of the imaging member 110. The reimageable surface may be formed of a relatively thin layer over a mounting layer, a thickness of the relatively thin layer being selected to balance printing or marking performance, durability, and manufacturability.

In some embodiments, the Imaging member 110 is used to apply an inked image to an image receiving media substrate 114 at a transfer nip 112. The transfer nip 112 may be formed by an impression roller 118, as part of an image transfer mechanism 160, exerting pressure in the direction of the imaging member 110. Image receiving medium substrate 114 should not be considered to be limited to any particular composition, such as; for example, paper, plastic, or composite sheet film. The exemplary printing system 100 may be used for producing images on a wide variety of image receiving media substrates 114. The 714 application also explains the wide latitude of marking (printing) materials that may be used, including marking materials with pigment densities greater than 10% by weight. As does the 714 application, this disclosure will use the term ink to refer to a broad range of printing or marking materials to include those which are commonly understood to be inks, pigments, and other materials which may be applied by the exemplary system 100 to produce an output image on the image receiving media substrate 114.

The 714 application depicts and describes details of the imaging member 110 including the imaging member 110 being comprised of a reimageable surface layer formed over a structural mounting layer that may be, for example, a cylindrical core, or one or more structural layers over a cylindrical core.

The exemplary printing system 100 may include a dampening fluid system 120 generally comprising a series of rollers, which may be considered as dampening rollers or collectively as a dampening unit, for uniformly wetting the reimageable surface of the imaging member 110 with dampening fluid. One purpose of the dampening fluid system 120 is to deliver a layer of dampening fluid, generally having a uniform and controlled thickness, to the reimageable surface of the imaging member 110. A dampening fluid such as fountain solution may comprise mainly water optionally with small amounts of isopropyl alcohol or ethanol added to reduce surface tension as well as to lower evaporation energy necessary to support subsequent laser patterning, as will be described in greater detail below. Small amounts of certain surfactants may be added to the fountain solution as well. Alternatively, other suitable dampening fluids may be used to enhance the performance of ink based digital lithography systems. Extensive experimentation has found that a preferred dampening fluid may be D4 (octamethylcyclotetrasiloxane). Other suitable dampening fluids are disclosed, by way of example, in U.S. patent application Ser. No. 13/284,114, filed on Oct. 28, 2011, titled “Dampening Fluid for Digital Lithographic Printing,” the disclosure of which is hereby incorporated herein by reference in its entirety.

Once the dampening fluid is metered onto the reimageable surface of the imaging member 110 by the dampening fluid system 120, a thickness of the dampening fluid may be measured using a sensor 125 that may provide feedback to control the metering of the dampening fluid onto the reimageable surface of the imaging member 110 by the dampening fluid system 120.

After an amount of dampening fluid is provided by the dampening fluid system 120 on the reimageable surface of the imaging member 110, an optical pattering subsystem 130 may be used to selectively form a latent image in the uniform dampening fluid layer by image-wise patterning the dampening fluid layer using, for example, laser energy. Typically, the dampening fluid will not absorb the optical energy (IR or visible) efficiently. The reimageable surface of the imaging member 110 should ideally absorb most of the laser energy (visible or invisible such as IR) emitted from the optical patterning subsystem 130 close to the surface to minimize energy wasted in heating the dampening fluid and to minimize lateral spreading of heat in order to maintain a high spatial resolution capability. Alternatively, an appropriate radiation sensitive component may be added to the dampening fluid to aid in the absorption of the incident radiant laser energy. While the optical patterning subsystem 130 is described above as being a laser emitter, it should be understood that a variety of different systems may be used to deliver the optical energy to pattern the dampening fluid.

The mechanics at work in the patterning process undertaken by the optical patterning subsystem 130 of the exemplary system 100 are described in detail with reference to FIG. 5 in the 714 application. Briefly, the application of optical patterning energy from the optical patterning subsystem 130 results in selective removal of portions of the layer of dampening fluid.

Following patterning of the dampening fluid layer by the optical patterning subsystem 130, the patterned layer over the reimageable surface of the imaging member 110 is presented to an inker subsystem 140. The inker subsystem 140 is used to apply a uniform layer of ink over the layer of dampening fluid and the reimageable surface layer of the imaging member 110. The inker subsystem 140 may use an anilox roller to meter an offset lithographic ink onto one or more ink forming rollers that are in contact with the reimageable surface layer of the imaging member 110. Separately, the inker subsystem 140 may include other traditional elements such as a series of metering rollers to provide a precise feed rate of ink to the reimageable surface of the Imaging member 110. The inker subsystem 140 may deposit the ink to the pockets representing the imaged portions of the reimageable surface, while ink on the unformatted portions of the dampening fluid will not adhere to those portions.

The cohesiveness and viscosity of the ink residing in the reimageable layer of the imaging member 110 may be modified by a number of mechanisms. One such mechanism may involve the use of a pre-cure or rheology (complex viscoelastic modulus) control subsystem 150. The rheology control system 150 may form a partial crosslinking core of the ink on the reimageable surface to, for example, increase ink cohesive strength relative to the reimageable surface layer. Curing mechanisms may include optical or photo curing, heat curing, drying, or various forms of chemical curing. However, in some embodiments, the cohesiveness and viscosity characteristics of the ink composition may not require pre-curing. For example, an acrylate ink composition may be delivered from the inker subsystem 140 to the image receiving medium 114 without partial pre-curing in-between. In some embodiments, cooling may be used to modify rheology as well via multiple physical cooling mechanisms, as well as via chemical cooling. For example, in one embodiment, the image receiving medium 114 or the impression roller 118 may be cooled.

In some embodiments, the use of an acrylate ink composition according to embodiments described herein may enable high transfer efficiency without the use of control subsystem 150, due to rheology and/or characteristics of the ink composition. For example, in some embodiments, a high viscosity and high tack of the ink composition enables transfer without pre-curing.

The ink is transferred from the reimageable surface of the imaging member 110 to a substrate of image receiving medium 114 using a transfer subsystem 160. The transfer occurs as the image receiving media substrate 114 is passed through a nip 112 between the imaging member 110 and an impression roller 118 such that the ink within the voids of the reimageable surface of the imaging member 110 is brought into physical contact with the image receiving media substrate 114. With the adhesion of the ink having been modified by the rheology control system 150, or the adhesion of the ink promoted based on a composition of the ink, adhesion of the ink may cause the ink to adhere to the image receiving media substrate 114 and to separate from the reimageable surface of the imaging member 110. Careful control of the rheology of the ink through composition or other means, as well as temperature and pressure conditions at the transfer nip 112, may allow, or otherwise facilitate, transfer efficiencies for the ink from the reimageable surface of the imaging member 110 to the image receiving media substrate 114 to exceed 95%. While it is possible that in some embodiments some dampening fluid may also wet the image receiving media substrate 114, the volume of such a dampening fluid will be minimal, and will rapidly evaporate or be absorbed by the image receiving media substrate 114.

In some embodiments, a temperature difference between delivery of the ink from the inker subsystem 140 to the image member 110 and delivery to the image receiving media substrate 114 enables transfer without pre-curing.

In certain offset lithographic systems, it should be recognized that an offset roller, not shown in FIG. 1, may first receive the inked image pattern and then transfer the inked image pattern to a substrate according to a known indirect transfer method.

Following the transfer of a high percentage of the ink to the image receiving media substrate 114, residual ink and/or residual dampening fluid should be removed from the reimageable surface of the imaging member 110, preferably without scraping or wearing the reimageable surface. For example, an air knife may be employed to remove residual dampening fluid and/or ink. It is anticipated, however, that some amount of ink residue may remain on the reimageable surface. Removal of such remaining ink residue may be accomplished through use of some form of cleaning subsystem 170. The 714 application describes details of such a cleaning subsystem 170 including at least a first cleaning member such as a sticky or tacky member in physical contact with the reimageable surface of the imaging member 110, the sticky or tacky member removing residual ink and any remaining small amounts of surfactant compounds from the reimageable surface of the imaging member 110. The sticky or tacky member may then be brought into contact with a smooth roller to which residual ink may be transferred from the sticky or tacky member, the ink being subsequently stripped from the smooth roller by, for example, a doctor blade.

The 714 application details other mechanisms by which cleaning of the reimageable surface of the imaging member 110 may be facilitated. Regardless of the cleaning mechanism, however, in some embodiments cleaning of the residual ink and dampening fluid from the reimageable surface of the imaging member 110 is needed to preventing ghosting in the proposed system. Once cleaned, the reimageable surface of the imaging member 110 is again presented to the dampening fluid system 120 by which a fresh layer of dampening fluid is supplied to the reimageable surface of the imaging member 110, and the process is repeated.

The imaging member reimageable surface may preferably be formed of a polymeric elastomer, such as silicone rubber and/or fluorosilicone rubber. The term “silicone” is well understood to those of skill in the relevant art and refers to polyorganosiloxanes having a backbone formed from silicon and oxygen atoms and sidechains containing carbon and hydrogen atoms. For the purposes of this application, the term “silicone” should also be understood to exclude siloxanes that contain fluorine atoms, while the term “fluorosilicone” is used to cover the class of siloxanes that contain fluorine atoms. Other atoms may be present in the silicone rubber, for example nitrogen atoms in amine groups which are used to link siloxane chains together during crosslinking. The side chains of the polyorganosiloxane can also be alkyl or aryl.

As discussed above, inks that are useful for ink-based digital offset printing must possess physical and chemical properties that meet the specific demands of ink-based digital printing systems such as the system shown in FIG. 1. The digital offset ink must be compatible with materials with which it is intended to come in contact, including the imaging plate (reimageable surface of the imaging member) and various dampening fluids, as well as printable substrates such as paper, metal, or plastic. The digital offset ink must also meet all functional requirements of the subsystems as imposed by wetting and transfer properties defined by subsystem architecture and materials sets.

In some embodiments, inks formulated for ink-based digital printing, or digital offset inks, are different in many ways from inks developed for other printing applications, including pigmented solvent inks, offset inks, flexography inks, UV gel inks, and the like. For example, digital offset inks contain much higher pigment loading leading to higher viscosities at room temperature than other inks, which can make ink delivery by way of an anilox roller system difficult. In some embodiments, digital offset inks should not cause the imaging member (reimageable) surface, which may be a silicone, fluorosilicone, or VITON-containing imaging plate or blanket, to swell and should be compatible with dampening fluid options.

Acrylate ink composition according to the embodiments disclosed herein have been found to minimize a solubility of the acrylate ink compositions in dampening fluid, such as D4, and to minimize or prevent swelling of a fluorosilicone-containing imaging member. Acrylate ink compositions in accordance with embodiments preferably exhibit a rheology that is suitable for anilox roller delivery. Acrylate ink compositions in accordance with some embodiments herein include digital offset acrylate inks that exhibit desirable transferability without pre-curing. In addition, some embodiments of the acrylate ink compositions are compatible with non-aqueous dampening fluids and exhibit desirable releasability from the imaging member (reimageable) surface after ink image formation.

In some embodiments, the acrylate ink compositions may include a pigment, an acrylate, a dispersant, and a photo initiator. In other embodiments, the acrylate ink compositions may also include a rheology modifier, and/or stabilizer.

For example, in one embodiment, the acrylate ink compositions may include pigments such as HELIOGEN Blue D 7088 available from BASF, Permanent Rubine L5B 01 (PR57:1), Permanent Yellow G-MX (PY 14), or HOSTAPERM Blue B4G, available from Clariant Corporation. Other suitable pigments include black pigments, white pigments, cyan pigments, magenta pigments, yellow pigments, and the like. Further, pigments may be organic or inorganic particles. Suitable inorganic pigments may include carbon black. However, other inorganic pigments may be suitable such as titanium oxide, and iron oxide. Suitable organic pigments include, for example, azo pigments including diazo pigments and monoazo pigments, polycyclic pigments (e.g., phthalocyanine pigments such as phthalocyanine blues and phthalocyanine greens), perylene pigments, perinone pigments, anthraquinone pigments, quinacridone pigments, dioxazine pigments, thioindigo pigments, isoindolinone pigments, pyranthrone pigments, and quinophthalone pigments), insoluble dye chelates (e.g., basic dye type chelates and acidic dye type chelate), nitro pigments, nitroso pigments, anthanthrone pigments such as PR168, and the like.

Representative examples of phthalocyanine blues and greens include copper phthalocyanine blue, copper phthalocyanine green, and derivatives thereof (Pigment Blue 15, Pigment Green 7, and Pigment Green 36). Representative examples of quinacridones include Pigment Orange 48, Pigment Orange 49, Pigment Red 122, Pigment Red 192, Pigment Red 202, Pigment Red 206, Pigment Red 207, Pigment Red 209, Pigment Violet 19, and Pigment Violet 42. Representative examples of anthraquinones include Pigment Red 43, Pigment Red 194, Pigment Red 177, Pigment Red 216 and Pigment Red 226. Representative examples of perylenes include Pigment Red 123, Pigment Red 149, Pigment Red 179, Pigment Red 190, Pigment Red 189 and Pigment Red 224. Representative examples of thioindigoids include Pigment Red 86, Pigment Red 87, Pigment Red 88, Pigment Red 181, Pigment Red 198, Pigment Violet 36, and Pigment Violet 38. Representative examples of heterocyclic yellows include Pigment Yellow 1, Pigment Yellow 3, Pigment Yellow 12, Pigment Yellow 13, Pigment Yellow 14, Pigment Yellow 17, Pigment Yellow 65, Pigment Yellow 73, Pigment Yellow 74, Pigment Yellow 90, Pigment Yellow 110, Pigment Yellow 117, Pigment Yellow 120, Pigment Yellow 128, Pigment Yellow 138, Pigment Yellow 150, Pigment Yellow 151, Pigment Yellow 155, and Pigment Yellow 213. Such pigments are commercially available in either powder or press cake form from a number of sources including, BASF Corporation, Engelhard Corporation, and Sun Chemical Corporation.

Examples of black pigments that may be used include carbon pigments. The carbon pigments may be almost any commercially available carbon pigment that provides acceptable optical density and print characteristics. Carbon pigments suitable for use in systems and methods in accordance with embodiments may include, without limitation, carbon black, graphite, vitreous carbon, charcoal, and combinations thereof. Such carbon pigments can be manufactured by a variety of known methods, such as a channel method, a contact method, a furnace method, an acetylene method, or a thermal method, and are commercially available from such vendors as Cabot Corporation, Columbian Chemicals Company, Evonik, Orion Engineered Carbons, and E.I. DuPont de Nemours and Company. Suitable carbon black pigments include, without limitation, Nipex 150 (available from Orion Engineered Carbons), Cabot pigments such as MONARCH 1400, MONARCH 1300, MONARCH 1100, MONARCH 1000, MONARCH 900, MONARCH 880, MONARCH 800, MONARCH 700, CAB-O-JET 200, CAB-O-JET 300, REGAL, BLACK PEARLS, ELFTEX, MOGUL, and VULCAN pigments; Columbian pigments such as RAVEN 5000, and RAVEN 3500; Orion Engineered Carbons pigments, such as Color Black FW 200, FW 2, FW 2V, FW 1, FW18, FW S160, FW S170, Special Black 6, Special Black 5, Special Black 4A, Special Black 4, PRINTEX U, PRINTEX 140U, PRINTEX V, and PRINTEX 140V. The above list of pigments includes unmodified pigment particulates, small molecule attached pigment particulates, and polymer-dispersed pigment particulates. Other pigments can also be selected, as well as mixtures thereof. In some embodiments, the pigment particle size is desired to be as small as possible to enable a stable colloidal suspension of the particles in the liquid vehicle, for example.

In one embodiment, the acrylate ink composition includes 30% or less pigment by weight, based on a total weight of the acrylate ink composition. In another embodiment, the acrylate ink composition includes 20% or less pigment. In another example, the acrylate ink composition includes between 10% and 20% pigment. In yet another example, the acrylate ink composition includes between 12% and 18% pigment. In another embodiment, the acrylate ink composition includes between 15% and 20% pigment. In another example, the acrylate ink composition includes 15% or 17.5% pigment.

In some embodiments, the acrylate ink compositions may include an acrylate. Acrylates or propenoates are salts and esters of acrylic acid. Acrylate and methacrylate monomers are understood to contain reactive vinyl functional groups that facilitate formation of acrylate polymers. Exemplary acrylates may include acrylate monomers, oligomers, or polymers, such as, difunctional monomers, for example, Sartomer SR247, Sartomer CD595 and Sartomer SR9003, trifunctional monomers, for example, Sartomer SR492, Sartomer SR9020, Sartomer SR501, Sartomer SR454 and Sartomer SR9035, and polyester acrylates, for example, Sartomer CN294E, Sartomer CN2282, Sartomer CN2295, Sartomer CN2264, Sartomer CN2256, and from AIInex, EBECRYL 450, EBECRYL 657 and EBECRYL 809.

In one embodiment, the acrylate ink composition includes between 40% and 80% acrylate by weight, based on a total weight of the acrylate ink composition. In another embodiment, the acrylate ink composition includes between 50% and 75% by weight acrylate. In yet another example, the acrylate ink composition includes between 60% and 70% by weight acrylate. In one example, the acrylate ink composition includes between 65% and 70% acrylate.

In some embodiments, the acrylate ink compositions may include a dispersant. The dispersants may include polymeric dispersants, such as those from Lubrizol including SOLSPERSE 32000, SOLSPERSE 39000, SOLSPERSE 71000, SOLSPERSE 78000, SOLSPERSE J-100, SOLSPERSE J-180, SOLSPERSE J-200, SOLSPERSE X300, and from BASF, such as EFKA 4300, EFKA 4330, EFKA 4340, EFKA 4400, EFKA PX 4701, EFKA 4585, EFKA 5207, EFKA 6230, EFKA 7701, EFKA 7731, and from Tego, such as TEGO Dispers 656, TEGO Dispers 685, TEGO Dispers 710, and from King Industries, such as K-SPERSE A-504.

In one embodiment, the acrylate ink composition includes 10% or less dispersant by weight, based on a total weight of the acrylate ink composition. In another example, the acrylate ink composition includes between 2% and 10% dispersant. In yet another example, the acrylate ink composition includes between 4% and 8% dispersant.

In some embodiments, the acrylate ink compositions may include rheology modifiers. Exemplary rheology modifiers may be modified or unmodified inorganic compounds including organodays, attapulgite clays and bentonite clays, including tetraallkyl ammonium bentonites as well as treated and untreated synthetic silicas. Suitable organodays include from Southern Clay Products CLAYTONE HA and CLAYTONE HY. Suitable examples of tetraallkyl ammonium bentonites include from Celeritas Chemicals CELCHEM 31743-09, CELCHEM 31744-09, and CELCHEM 31745-09. Other exemplary rheology modifiers include organic compounds such as EFKA RM1900 and EFKA RM1920, both modified hydrogenated castor oils from BASF.

In one embodiment, the acrylate ink composition includes 12% or less rheology modifiers by weight, based on a total weight of the acrylate ink composition. In another example, the acrylate ink composition includes between 1% and 5% rheology modifiers. In yet another example, the acrylate ink composition includes 3% or less rheology modifiers. In one embodiment, the acrylate ink composition includes 2% rheology modifiers.

In some embodiments, the acrylate ink compositions may include photoinitiators. Photoinitiators may be liquid- or solid-based or combinations thereof. Suitable Type I photoinitiators include those from classes of dialkoxy-aceto-pheonones, dialkoxy-alkyl-pheonones, amino-alkyl-pheonones, and acyl-phosphine oxides. Suitable Type II photoinitiators include those from classes of benzophenones and thioxanthones, which require activation from suitable amine synergists. Exemplary photoinitiators include ADDITOL LX, ADDITOL DX, ADDITOL BDK, ADDITOL CPK, ADDITOL DMMTA, ADDITOL TPO from Alinex, Esacure 1001M from IRGACURE 127, IRGACURE 184, IRGACURE 379, IRGACURE 819 and IRGACURE 2959 from BASF. Exemplary amine synergists that are used with Type II photoinitiators include SPEEDCURE PDA, SPEEDCURE EDB from Lambson, Diethylaminoethyl Methacrylate, Ethyl-4-dimethylamino benzoate, 2-Ethylhexyl 4-dimethylamino benzoate from Esstech, Inc. In some embodiment, the acrylate ink composition may include low odor photoinitiators, such as, ESACURE KIP 150 available from Lamberti S.p.A.

In one embodiment, the acrylate ink composition includes 12% or less photoinitiators by weight, based on a total weight of the acrylate ink composition. In another example, the acrylate ink composition includes 10% or less photoinitiators. In yet another example, the acrylate ink composition includes between 5% and 10% photoinitiators. In one embodiment, the acrylate ink composition includes between 6% and 8% by weight photoinitiators.

In some embodiments, the acrylate ink compositions may stabilizers. In some embodiments, the stabilizers may be embodied as a free radical polymerization inhibitor or a free radical scavenger. In some embodiments, the stabilizer offers stability against pre-mature partial polymerization of the acrylate ink composition. For example, the stabilizers may include Sartomer USA CN3216 (an active component proprietary stabilizer with p-methoxyphenol in a proprietary acrylate monomer and a proprietary acrylate oligomer), BASF IRGASTAB UV22 (a hindered phenol), and GENORAD 16 and GENORAD 18, both from Rahn USA Corporation.

In one embodiment, the acrylate ink composition includes 1.5% or less active component stabilizers by weight, based on a total weight of the acrylate ink composition. In another example, the acrylate ink composition includes 0.4% or less stabilizers. In another example, the acrylate ink composition includes between 0.1% and 0.3% stabilizers. In one embodiment, the acrylate ink composition includes 0.2% stabilizers.

Acrylate ink compositions in accordance with the embodiments described herein may be formed by preparing an ink base and mixing it with one or more of the components recited above.

Aspects of the present disclosure may be further understood by referring to the following examples. The examples are illustrative, and are not intended to be limiting embodiments thereof. Examples 1-4 illustrate embodiments of acrylate ink compositions according to the disclosure.

Example 1

Based on a total 400 gram scale of preparation for a cyan ink composition, 4.5% wt. of SOLSPERSE 39000, 65% wt. of CN294E, 5.49% of CD501, and 1% wt. of CN3216 were added to a 1 liter stainless steel vessel and placed on a heating mantle (available from IKA®) together with a thermocouple and stirrer apparatus (also available from IKA®) and equipped with an anchor impeller. The components in the vessel (dispersant, acrylates, and stabilizer) were then stirred at 200 RPM for 30 minutes at 80° C. Thereafter photoinitiators (2% wt. Irgacure 379, 0.39% wt. Irgacure 819, 1% wt. Irgacure 184, and 3.62% wt. Esacure Kip 150) were added slowly to the vessel and stirred at about 80° C. for another hour. With the components in the vessel solubilized, 15% wt. of Heliogen Blue D 7088 pigment was added to the vessel and stirred more vigorously but not to the point where air was entrained into the mixture. The pigmented mixture was allowed to stir for about 30 minutes at about 400 RPM at which point 2% wt. Claytone HY was added slowly to the pigmented mixture at a reduced RPM and then re-stirred for about another 15 minutes at about 400 RPM. The vessel containing the mixed components was then transferred to a high speed shearing mill (available from the Hockmeyer Equipment Corporation) equipped with a 40 mm diameter high shear Cowles blade and stirred at 5300 RPM for about an hour to form COMPONENT MIXTURE 1A. COMPONENT MIXTURE 1A was then qualitatively transferred to a 3-roll mill apparatus (manufactured by Kent Machine Works) where COMPONENT MIXTURE 1A was passed through the 3-roll mill first at an input apron roll speed of 400 RPM for a first pass and then at an input apron roll speed of 200 RPM for a second pass to form COMPONENT MIXTURE 1B forming the Example 1 acrylate ink composition.

Example 2

An acrylate ink composition was prepared in the same manner as Example 1 using a magenta pigment and the components percentages detailed in Table 1.

Example 3

An acrylate ink composition was prepared in the same manner as Example 1 using a yellow pigment and the components percentages detailed in Table 1.

Example 4

An acrylate ink composition was prepared in the same manner as Example 1 using a different cyan pigment and the components percentages detailed in Table 1.

Table 1 summarizes the component and percentages of the acrylate ink compositions in Examples 1-4.

TABLE 1

Formulation of Example Inks

Ink Composition Formulation

	Available
Component	from	Example 1	Example 2	Example 3	Example 4

Pigment	HELIGOEN	BASF		15	—	—	—
	Blue D 7088
	Permanent	Clariant	—	15	—	—
	Rubine L5B 01	Corp.
	(PR57:1)
	Permanent	Clariant	—	—	17.5	—
	Yellow G-MX	Corp.
	(PY 14)
	HOSTAPERM	Clariant	—	—	—	17.5
	Blue B4G	Corp.
Dispersant	Solsperse	Lubrizol	4.5	—	—	7
	39000	Corp.
	Solsperse J-180	Lubrizol	—	6	4.8	—
		Corp.
Oligomer	CN294E	Sartomer Co.	65	48.91	57.41	61.73
	CN2256	Sartomer Co.	—	8.81	4.5	—
Monomer	CD501	Sartomer Co.	5.49	11.27	5.8	1.76
Photoinitiator	Irgacure 379	BASF	2	2	2	2
	Irgacure 819	BASF	0.39	0.39	0.39	0.39
	Irgacure 184	BASF	1	1	1	1
	Esacure KIP	Lamberti	3.62	3.62	3.60	3.62
	150	Technologies
Stabilizer	CN3216	Sartomer Co.	1	1	1	1
Rheology	Claytone HY	Southern		2	2	2	4
Modifier		Clay
		Products

Total Weight Percentage	100	100	100	100

The ink composition of Examples 1-4 were analyzed in terms of rheology and tack. In particular, the frequency-based sweep rheologies, between applied 0.1 and 100 rad/s frequencies, of all inks were determined on a RFS-3 rheometer (available from TA Instruments) at 25° C., 35° C., and 45° C. equipped with a 25 mm plate at a 0.5 mm gap. The rheology results of the inks can be found in Table 2 below.

TABLE 2

Rheology Results (Complex Viscosities in cP)

Complex
Viscosity	Example 1	Example 2
Frequency	complex viscosity (cP)	complex viscosity (cP)

(rad/s)	25° C.	35° C.	45° C.	25° C.	35° C.	45° C.

1.00	1.04E+06	9.87E+05	6.34E+06	—	5.58E+05	5.91E+04
2.51	7.31E+05	5.76E+05	3.50E+05	—	3.65E+05	4.79E+04
6.31	5.38E+05	3.54E+05	2.06E+05	—	2.50E+05	4.05E+04
10.00	4.70E+05	2.88E+05	1.61E+05	—	2.12E+05	3.74E+04
25.12	3.63E+05	1.91E+05	1.02E+05	—	1.55E+05	3.15E+04
100.00	2.24E+05	1.02E+05	5.05E+04	—	9.06E+04	2.22E+04

Complex
Viscosity	Example 3	Example 4
Frequency	complex viscosity (cP)	complex viscosity (cP)

(rad/s)	25° C.	35° C.	45° C.	25° C.	35° C.	45° C.

1.00	2.03E+06	2.10E+06	1.64E+06	—	1.10E+06	6.12E+05
2.51	1.28E+06	1.08E+06	7.80E+05	—	6.38E+05	3.34E+05
6.31	8.85E+05	6.05E+05	3.91E+05	—	3.92E+05	1.92E+05
10.00	7.55E+05	4.69E+05	2.85E+05	—	3.16E+05	1.49E+05
25.12	5.62E+05	2.94E+05	1.58E+05	—	2.10E+05	9.22E+04
100.00	3.20E+05	1.45E+05	6.85E+04	—	1.10E+05	4.53E+04

According to the values Illustrated in Table 2, energy of activation for viscous flow for the various acrylate ink compositions were calculated by determining the slope of an Arrhenius plot of the natural logarithm of complex viscosity (for the selected frequencies) and the reciprocal absolute temperature in Kelvins. The data is presented in Table 3 in terms of KJ/mol. It should be noted that the units of KJ/mol are typically used for materials including solvents, co-solvents, single component crystalline or amorphous materials. The units KJ/mol for heterogeneous systems such as the acrylate ink compositions of Table 3 can be thought of as the normalized energy of activation for viscous flow of a given ink composition formulated within a certain compositional boundary.

TABLE 3

Energies of Activation for Viscous Flow
Energy of Activation at 100 rad/s (KJ/mol)

Example 1	Example 2	Example 3	Example 4

58.7	107.3	60.8	67.6

In some embodiments, the energy of activation at specific frequencies correlates with a viscosity sensitivity to temperature property of the ink compositions. For example, in some embodiments, if the energy of activation is too high, the ink composition will not flow well, and if the energy of activation is too low, the ink composition will be too fluid. In some embodiments, the ability of an ink composition to transfer at a higher temperature to an Anilox roller and then to set upon an imaging plate can be predicted from their energy of activation at specific frequencies. In one embodiment, the acrylate ink compositions have an energy of activation of between 40 and 120 at 100 rad/s. In another embodiment, the acrylate ink compositions have an energy of activation of between 50 and 110 at 100 rad/s. In yet another embodiment, the acrylate ink compositions have an energy of activation of between 55 and 80 at 100 rad/s.

Accordingly, embodiments in the present disclosure provide ink compositions which maintain a preferred rheology at one temperature while simultaneously maintaining a preferred range of energy of activation. FIG. 2 illustrates the frequency-based rheograms of the ink compositions of Examples 1-4 at 35° C. As illustrated in FIG. 2, the complex viscosity of the ink compositions is within 80,000 cP and 170,000 cP at 35° C.

Similarly, each of the ink compositions in Examples 1-4 was tested on an Inkometer 1100 (available from Thwing-Albert Company) to determine tack. The UV ink-rated rollers on the Inkometer were equilibrated at 32.2° C. In each case, 1.3 mL of the ink composition was applied to the distribution roller where transfer and distribution on to the other rollers was allowed to continue for 15 seconds at 150 RPM upon which time the speed of the rollers was automatically increased to 1200 RPM. Tack measurements of the ink occurred every 20 seconds for 10 minutes, the 60 second tack results can be found in FIG. 3 in terms of grams-meters.

As illustrated in FIG. 3, the 60 second tack dependence is approximately linear for Examples 1-4 at temperatures less than about 40° C. However, the inventors have discovered there is a surprising and unexpected departure from what can be considered a first-order relationship between tack and temperature among the Example Inks at temperatures above 40° C. For example, in some embodiments, the ink compositions have a tack that is unexpectedly higher at temperatures at and near 50° C. and potentially above 50° C. In some embodiments, acrylate ink compositions have a tack measurement of between 15 g-m and 30 g-m at 60 seconds at 50° C. In another embodiment, the acrylate ink compositions have a tack measurement of between 18 and 28 g-m at 60 seconds at 50° C. In one embodiment, the acrylate ink composition has a tack measurement of 25 g-m at 60 seconds at 50° C.

Accordingly, in some embodiments, the acrylate ink compositions in the disclosure have a lower viscosity at elevated temperatures to enable better fill-in of the ink composition in the Anilox delivery roller, while simultaneously displaying a high tack to allow for the successful transfer of the ink composition from the Anilox roller to the imaging plate, resulting in a higher and more uniform optical densities of the imaged ink on the printing substrate.

In some embodiments, the acrylate ink composition has a high viscosity and high tack at or near room temperature. In one embodiment, the high viscosity/high tack state enables transfer of the acrylate ink composition without the use of pre-cure step. In some embodiments, at temperatures above ambient room temperature, such as about 40° C., about 50° C., and about 60° C., the viscosity of the ink composition is lower to enable ink delivery and wetting onto the imaging blanket while also having sufficient tack at these elevated temperature to maintain adequate ink cohesion for effective and consistent ink transfer and image uniformity. In one embodiment, the acrylate ink composition has a tack between 20-35 g-m, at elevated temperatures of about 40° C. to about 70° C.

Accordingly, in some embodiments, the acrylate ink composition has a near-zero shear viscosity of between 2×10⁶and 5×10⁷cps at 25° C. and a near zero shear viscosity of between 2×10⁵to 4×10⁶cps at 60° C.

In one embodiment, the acrylate ink composition has a near-zero shear viscosity of between 4×10⁶and 1×10⁷cps at 25° C. and a near zero shear viscosity of between 4×10⁵to 8×10⁵cps at 60° C.

In other embodiments, the acrylate ink composition has a 60 second tack of between 40-65 g-m at 25° C.; a 60 second tack of between 30-50 g-m at 32° C.; a 60 second tack of between 25-35 g-m at 40° C.; a 60 second tack of between 15-30 g-m at 50° C.; and a 60 second tack of between 10-20 g-m at 60° C.

In one embodiment, the acrylate ink composition has a 60 second tack of between 45-55 g-m at 25° C.; a 60 second tack of between 35-50 g-m at 32° C.; a 60 second tack of between 25-30 g-m at 40° C.; a 60 second tack of between 20-25 g-m at 50° C.; and a 60 second tack of between 10-15 g-m at 60° C.

In one embodiment, when the ink composition is part of a set of ink compositions, each ink composition may have a minimum differential tack to allow full transfer of the ink composition to the substrate. For example, in one embodiment, each ink composition may have a tack differential of between 2 and 5 g-m.

In some embodiments, acrylate ink compositions with a higher tack are beneficial for increased ink transfer and image quality when used in printing systems, such as digital lithographic printing systems.

In some embodiments, the higher tack and lower rheology of acrylate ink compositions at certain temperatures allow efficient transfer of images from the imaging plate to a substrate without a pre-cure option.

In some embodiment, the acrylate ink composition is applied to a reimageable surface of an imaging member at a first temperature; and the acrylate ink composition is transferred to a substrate at a second temperature. In some embodiment, the temperature difference between the first temperature and the second temperature is at least 20° C. In other embodiments, the temperature difference between the first temperature and the second temperature is at least 30° C. In another embodiment, the temperature difference between the first temperature and the second temperature is at least 40° C. In another embodiment, the temperature difference between the first temperature and the second temperature is at least 50° C. In another embodiment, the temperature difference between the first temperature and the second temperature is at least 60° C. In another embodiment, the temperature difference between the first temperature and the second temperature is at least 70° C. In another embodiment, the temperature difference between the first temperature and the second temperature is at least 80° C. In some embodiments, the temperature difference between the first temperature and the second temperature is between 20° C. and 80° C.

In one embodiment, the first and second temperatures are in the range of 25° C. to 60° C., the second temperature is lower than the first temperature, and a 60 second tack of the acrylate ink composition Is about 1.3 times lower (+/−˜0.1) per 7 to 8° C. increase in temperature from the first temperature. In another embodiment, the first and second temperatures are in the range of 25° C. to 60° C., the second temperature is lower than the first temperature, and a near-zero shear viscosity of the acrylate ink composition is about 1.2 times lower (+/−˜0.1) per 10° C. increase in temperature from the first temperature.

In some embodiments, acrylate ink compositions in accordance with the embodiments of this disclosure are compatible with dampening fluids and imaging member or reimageable surface/plate materials of ink-based digital printing systems. For example, embodiments of the acrylate ink compositions may be immiscible in dampening fluids, such as D4, and provide low background in non-imaging areas.

The present disclosure has been described with reference to exemplary embodiments. Although a few embodiments have been shown and described, it will be appreciated by those skilled in the art that changes may be made in these embodiments without departing from the principles and spirit of preceding detailed description. It is intended that the present disclosure be construed as including all such modifications and alterations Insofar as they come within the scope of the appended claims or the equivalents thereof.

Claims

The invention claimed is:

1. An ink composition, comprising:

20% or less by weight pigment, based on a total weight of the ink composition;

10% or less by weight dispersant, based on the total weight of the ink composition;

between 50% and 75% by weight acrylate, based on the total weight of the ink composition, wherein the acrylate comprises propoxylated (6) trimethylolpropane triacrylate, tetra-functional acrylated polyester oligomer and a high-viscosity di-functional acrylated polyester oligomer; and

between 5% and 10% by weight photoinitiator, based on the total weight of the ink composition,

wherein a near-zero shear viscosity of the ink composition is:

between 2×10⁶cP and 5×10⁷cP at 25° C., and

between 2×10⁵cP and 4×10⁶cP at 60° C., and

wherein a 60 second tack of the ink composition is:

between 40 g-m and 65 g-m at 25° C., and

between 10 g-m and 20 g-m at 60° C.

2. The ink composition of claim 1, further comprising:

1.5% or less by weight stabilizer, based on the total weight of the ink composition; and

12% or less by weight rheology modifier, based on the total weight of the ink composition.

3. The ink composition of claim 2, comprising:

between 15% and 20% pigment;

between 4% and 8% dispersant;

between 60% and 70% acrylate;

between 5% and 10% photoinitiator;

between 0.1% and 0.3% stabilizer; and

3% or less rheology modifier,

wherein the ink composition has a near-zero shear viscosity between 4×10⁶cP and 1×10⁷cP at 25° C., and between 4×10⁵cP and 8×10⁵cP at 60° C., and

wherein a 60 second tack of the ink composition is between 45 g-m and 55 g-m at 25° C., and between 10 g-m and 15 g-m at 60° C.

4. The ink composition of claim 3, wherein the acrylate further comprises at least one of an acrylate monomer, acrylate polymer, acrylate oligomer, a difunctional acrylate monomer, and mixtures thereof.

5. The ink composition of claim 1, wherein the high-viscosity di-functional acrylated polyester oligomer has a viscosity of at least 11,000 cps at 60° C.

6. An ink composition, essentially consisting of:

20% or less by weight pigment, based on a total weight of the ink composition;

between 50% and 75% by weight acrylate, based on the total weight of the ink composition,

wherein the acrylate comprises a trifunctional acrylate monomer and a high-viscosity, di-functional acrylated polyester oligomer; and,

optionally, one or more acrylates selected from the group consisting of an acrylate monomer, acrylate polymer, acrylate oligomer, and a difunctional acrylate monomer,

between 5% and 10% by weight photoinitiator, based on the total weight of the ink composition;

1.5% or less by weight stabilizer, based on the total weight of the ink composition;

and 12% or less by weight rheology modifier, based on the total weight of the ink composition,

wherein a near-zero shear viscosity of the ink composition is:

between 2×10⁶cP and 5×10⁷cP at 25° C., and

between 2×10⁵cP and 4×10⁶cP at 60° C.,

and wherein a 60 second tack of the ink composition is:

between 40 g-m and 65 g-m at 25° C., and

between 10 g-m and 20 g-m at 60° C.

7. The ink composition of claim 6, essentially consisting of:

between 15% and 20% pigment;

between 4% and 8% dispersant;

between 60% and 70% acrylate;

between 5% and 10% photoinitiator;

between 0.1% and 0.3% stabilizer; and

3% or less rheology modifier,

8. The ink composition of claim 6, wherein the high-viscosity di-functional acrylated polyester oligomer has a viscosity of at least 11,000 cps at 60° C.

9. A method of printing using a variable data digital lithographic printing device, comprising:

applying an ink composition to a reimageable surface of an imaging member; and

transferring the ink composition from the reimageable surface to a substrate, wherein the ink composition does not require pre-curing before transferring the ink composition from the reimageable surface to the substrate, wherein the ink composition comprises:

20% or less by weight pigment, based on a total weight of the ink composition;

wherein the acrylate comprises a trifunctional acrylate monomer and a high-viscosity, di-functional acrylated polyester oligomer

and optionally one or more acrylates selected from the group consisting of an acrylate monomer, acrylate polymer, acrylate oligomer, and a difunctional acrylate monomer,

12% or less by weight rheology modifier, based on the total weight of the ink composition,

wherein a near-zero shear viscosity of the ink composition is:

between 2×10⁶cP and 5×10⁷cP at 25° C., and between 2×10⁵cP and 4×10⁶cP at 60° C.

and wherein a 60 second tack of the ink composition is:

between 40 and 65 g-m at 25° C.,

and between 10 and 20 g-m at 60° C.

10. The method of claim 9, wherein the ink composition consists essentially of:

between 15% and 20% pigment;

between 4% and 8% dispersant;

between 60% and 70% acrylate;

between 5% and 10% photoinitiator;

between 0.1% and 0.3% stabilizer; and

3% or less rheology modifier;

wherein the ink composition has a near-zero shear viscosity between 4×10⁶cP and 1×10⁷cP at 25° C., and between 4×10⁵cP and 8×10⁵cP at 60° C., and wherein a 60 second tack of the ink composition is between 45 g-m and 55 g-m at 25° C., and between 10 g-m and 15 g-m at 60° C.

11. The method of claim 9, wherein the high-viscosity di-functional acrylated polyester oligomer has a viscosity of at least 11,000 cps at 60° C.

12. A method of printing using a variable data digital lithographic printing device, comprising:

applying an ink composition at a first temperature to a reimageable surface of an imaging member; and

transferring the ink composition from the reimageable surface to a substrate at a second temperature,

wherein the ink composition does not require pre-curing before transferring the ink composition from the reimageable surface to the substrate,

wherein the ink composition comprises:

20% or less by weight pigment, based on a total weight of the ink composition;

between 5% and 10% or less by weight photoinitiator, based on the total weight of the ink composition,

wherein a near-zero shear viscosity of the ink composition is

between 2×10⁶cP and 5×10⁷cP at 25° C., and

between 2×10⁵cP and 4×10⁶cP at 60° C., and

wherein a 60 second tack of the ink composition is

between 40 g-m and 65 g-m at 25° C., and

between 10 g-m and 20 g-m at 60° C.

13. The method of claim 12, wherein the composition comprises:

between 15% and 20% pigment;

between 4% and 8% dispersant;

between 60% and 70% acrylate;

between 5% and 10% photoinitiator;

between 0.1% and 0.3% stabilizer; and

3% or less rheology modifier,

14. The method of claim 13, wherein the acrylate further comprises at least one of an acrylate monomer, acrylate polymer, acrylate oligomer, a difunctional acrylate monomer, and mixtures thereof.

15. The method of claim 12, wherein the high-viscosity di-functional acrylated polyester oligomer has a viscosity of at least 11,000 cps at 60° C.